Synthesis of benzothiazine sulfonamides via heteroatomic Diels-Alder reaction of para-fluoro-N-sulfinylaniline with bicyclo[2.2.1]heptenes

dc.contributor.author	Veremeichik Y.
dc.contributor.author	Shurpik D.
dc.contributor.author	Lodochnikova O.
dc.contributor.author	Plemenkov V.
dc.date.accessioned	2018-09-19T21:00:19Z
dc.date.available	2018-09-19T21:00:19Z
dc.date.issued	2016
dc.identifier.issn	1070-3632
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/143498
dc.description.abstract	© 2016 Pleiades Publishing, Ltd.Reaction of 4-fluoro-N-sulfinylaniline with norbornene and norbornadiene has afforded the Diels-Alder adducts of benzothiazine structure that have been oxidized into the corresponding benzothiazine sulfonamides. Structure of the obtained compounds and stereochemistry of the diene addition and epoxidation of norbornene olefin bonds have established by means of X-ray diffraction method.
dc.relation.ispartofseries	Russian Journal of General Chemistry
dc.subject	bicyclo[2.2.1]heptene
dc.subject	Diels-Alder reaction
dc.subject	fluoro-N-sulfinylaniline
dc.subject	sulfonamides
dc.title	Synthesis of benzothiazine sulfonamides via heteroatomic Diels-Alder reaction of para-fluoro-N-sulfinylaniline with bicyclo[2.2.1]heptenes
dc.type	Article
dc.relation.ispartofseries-issue	2
dc.relation.ispartofseries-volume	86
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	296
dc.source.id	SCOPUS10703632-2016-86-2-SID84964026727

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